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Journal Articles

Fracture Prevalence in Adults with Transfusion-Dependent Thalassemia Is Related to Osteoporosis and Age

John C. Chapin, MD, Maria Vogiatzi, MD, Dorothy Kleinert, NP, Ersilia DeFilippis, Paul Christos, DrPH, Patricia Giardina, MD

Blood (2014) 124 (21): 4902.

https://doi.org/10.1182/blood.V124.21.4902.4902

Published: 2014

Journal Articles

The Effect of Vitamin D Supplementation On Calcium Excretion in Thalassemia

Sadana Balachandar, MD, Rachel Randolph, BS, Dorothy A. Kleinert, NP, MPH, CPNP, Sujit Sheth, MD, Patricia Giardina, MD, Maria G Vogiatzi, MD

Blood (2012) 120 (21): 1029.

https://doi.org/10.1182/blood.V120.21.1029.1029

Published: 2012

Journal Articles

Removal of Macrophages From the Erythroid Niche Impairs Stress Erythropoiesis but Improves Pathophysiology of Polycythemia Vera and Beta-Thalassemia

Pedro Ramos, PhD, Carla Casu, PhD, Sara Gardenghi, PhD, Laura Breda, Ph.D, Bart J Crielaard, PhD, Ritama Gupta, Undergraduate student, Ella Guy, Maria F Mariongiu, PhD, Ross L. Levine, Omar Abdel-Wahab, PhD, Benjamin L. Ebert, Nico van Rooijen, PhD, Saghi Ghaffari, MD, PhD, Robert W Grady, PhD, Patricia Giardina, MD, Stefano Rivella, PhD

Blood (2012) 120 (21): 81.

https://doi.org/10.1182/blood.V120.21.81.81

Published: 2012

Journal Articles

Transfusion Complications in Thalassemia: A Report From the Centers for Disease Control and Prevention (CDC)

Elliott Vichinsky, MD, Lynne Neumayr, MD, Sean Trimble, MPH, Alexis A. Thompson, MD, MPH, Patricia Giardina, MD, Alan R. Cohen, MD, Thomas D. Coates, MD, Ellis J. Neufeld, MD, PhD, Althea M Grant, MPH, PhD, Jeanne Boudreaux, MD

Blood (2011) 118 (21): 340.

https://doi.org/10.1182/blood.V118.21.340.340

Published: 2011

Journal Articles

Potential Therapeutic Applications of Jak2 Inhibitors in Beta-Thalassemia and Sickle Cell Disease,

Carla Casu, PhD, Pedro Ramos, PhD, Luca Melchiori, PhD, Ella Guy, Eliezer A. Rachmilewitz, Patricia Giardina, MD, Robert W Grady, PhD, Maria de Sousa, MD, PhD, Stefano Rivella, PhD

Blood (2011) 118 (21): 3187.

https://doi.org/10.1182/blood.V118.21.3187.3187

Published: 2011

Journal Articles

Investigating the Role of Cytokines and Hepcidin in Anemia of Inflammation

Sara Gardenghi, PhD, Thomas M. Renaud, MD, Alessandra Meloni, PhD, Pedro Ramos, PhD, Carla Casu, PhD, Keegan S Cooke, Barbra J Sasu, PhD, Patricia Giardina, MD, Robert W Grady, PhD, Stefano Rivella, PhD

Blood (2011) 118 (21): 1046.

https://doi.org/10.1182/blood.V118.21.1046.1046

Published: 2011

Journal Articles

The Human Ankyrin Insulator Supports Production of Therapeutic Levels of Adult Hemoglobin Following β-Globin Gene Transfer in Hematopoietic Cells Derived From Thalassemic and Sickle Cell Patients

Laura Breda, PhD, Carla Casu, Nicoletta Bianchi, Luca Cartegni, Karina Yazdanbakhsh, PhD, Deepa Manwani, MD, Narla Mohandas, Petar Jelinic, Gregory David, Lawrence B. Gardner, MD, Dorothy A Kleinert, NP, MPH, Eugenia Prus, Eitan Fibach, PhD, Patricia Giardina, MD, Roberto Gambari, Stefano Rivella, PhD

Blood (2011) 118 (21): 2055.

https://doi.org/10.1182/blood.V118.21.2055.2055

Published: 2011

Journal Articles

Monitoring Cardiac Siderosis in Patients with Beta-Thalassemia Major on Various Chelation Regimens,

Srikanth R. Ambati, MBBS, MD, Rachel Randolph, B.S., Kevin Mennitt, MD, Dorothy A Kleinert, NP, MPH, Patricia Giardina, MD

Blood (2011) 118 (21): 3177.

https://doi.org/10.1182/blood.V118.21.3177.3177

Published: 2011

Journal Articles

Changes In Health Status and Quality of Life In Adults with Thalassemia: Year 1 Report of the Thalassemia Longitudinal Cohort Study.

Amy Sobota, MD, Robert Yamashita, Ph.D, Yan Xu, MS, Felicia Trachtenberg, PhD, Pamela Kohlbry, PhD, RN, Dorothy A Kleinert, NP, MPH, Patricia Giardina, MD, Janet L Kwiatkowski, MD, MSCE, Dru Haines, RN, CPNP, MSN, Vivekanandan Thayalasuthan, MD, John B. Porter, MA, MD, FRCP, FRCPath, Alexis A. Thompson, MD, MPH, Leann Schilling, MPH, Charles T. Quinn, MD, MS, Ellis J. Neufeld, MD, PhD

Blood (2010) 116 (21): 1533.

https://doi.org/10.1182/blood.V116.21.1533.1533

Published: 2010

Journal Articles

Therapeutic Transgene Expression From Genomic Safe Harbors In Patient-Specific Induced Pluripotent Stem Cells

Eirini P Papapetrou, MD, PhD, Gabsang Lee, PhD, Nirav Malani, Manu Setty, Isabelle Riviere, PhD, Laxmi MS Tirunagari, Kyuichi Kadota, MD, Shoshannah L Roth, PhD, Patricia Giardina, MD, Agnes Viale, PhD, Christina Leslie, PhD, Frederic Bushman, PhD, Lorenz Studer, MD, Michel Sadelain, MD, PhD

Blood (2010) 116 (21): 564.

https://doi.org/10.1182/blood.V116.21.564.564

Published: 2010

Journal Articles

The Palatability and Tolerability of Deferasirox (Exjade®) Taken with Meals, Different Liquids, or Crushed and Added to Food

Stuart L Goldberg, MD, Patricia Giardina, MD, Joan Parkhurst Cain, MD, Deborah Chirnomas, MD, MPH, Jason Esposito, Carole S. Paley, MD, Elliott Vichinsky, MD

Blood (2010) 116 (21): 5155.

https://doi.org/10.1182/blood.V116.21.5155.5155

Published: 2010

Journal Articles

Hepcidin as a Therapeutic Tool to Limit Iron Overload and Improve Anemia In β-Thalassemia

Sara Gardenghi, PhD, Pedro Ramos, Cindy N. Roy, PhD, Nancy C. Andrews, MD, PhD, Elizabeta Nemeth, PhD, Xiuli An, MD, PhD, Mohandas Narla, DSc, Yelena Ginzburg, MD, Eliezer A. Rachmilewitz, MD, Patricia Giardina, MD, Robert W Grady, Stefano Rivella, PhD

Blood (2010) 116 (21): 1009.

https://doi.org/10.1182/blood.V116.21.1009.1009

Published: 2010

Journal Articles

Changes In Health Status and Quality of Life In Parental Reports of Children with Thalassemia: Year 1 Report of the Thalassemia Longitudinal Cohort Study

Robert Yamashita, Ph.D, Amy Sobota, MD, Felicia Trachtenberg, PhD, Yan Xu, MS, Isaac Odame, Alexis A. Thompson, MD, MPH, Patricia Giardina, MD, Dru Haines, RN, CPNP, MSN, Zahra Pakbaz, MD, Dorothy A Kleinert, Charles T. Quinn, MD, MS, Janet L Kwiatkowski, MD, MSCE, Leann Schilling, MPH, Jeanne Boudreaux, MD, Ellis J. Neufeld, MD, PhD

Blood (2010) 116 (21): 257.

https://doi.org/10.1182/blood.V116.21.257.257

Published: 2010

Journal Articles

Understanding Provider Barriers to Hydroxyurea Use for Pediatric Sickle Cell Disease

Suzette O. Oyeku, MD, MPH, Nancy S. Green, MD, Farzana Pashankar, MD, Patricia Giardina, MD, Craig A. Mullen, MD, PhD, Catherine Driscoll, MD

Blood (2010) 116 (21): 255.

https://doi.org/10.1182/blood.V116.21.255.255

Published: 2010

Journal Articles

Genetics of HbF and HbF Response to Hydroxyurea In Pediatric Sickle Cell Disease: A Multi-Site Pilot Analysis of Candidate SNP Variants

Nancy S. Green, MD, Katherine Ender, MD, MPH, Farzana Pashankar, MD, Catherine Driscoll, MD, Patricia Giardina, MD, Craig A. Mullen, MD, PhD, Lorraine Clark, PhD, Jennifer Crotty, PNP, Mara Burney, RN, MPH, Carolyn Hoppe, MD, Sandra Barral, PhD

Blood (2010) 116 (21): 2641.

https://doi.org/10.1182/blood.V116.21.2641.2641

Published: 2010

Journal Articles

Phenomenon of Pain In Thalassemia: A Prospective Analysis by the Thalassemia Clinical Research Network (TCRN)

Blood (2010) 116 (21): 256.

https://doi.org/10.1182/blood.V116.21.256.256

Published: 2010

Journal Articles

Increased Nucleosomal DNA Fragmentation in Leukocytes of Thalassemia Patients.

Patrick B Walter, PhD, John B Porter, MD, Patricia Evans, PhD, Janet Kwiatkowski, MD, Ellis J. Neufeld, MD, PhD, Thomas D. Coates, MD, Patricia Giardina, MD, Robert jW Grady, PhD, Elliott Vichinsky, MD, Nancy F. Olivieri, MD, Felicia Trachtenberg, PhD, Daniele Alberti, MD, Ellen Fung, PhD, Bruce Ames, PhD, Annie Lui, BS, Paul Harmatz, MD

Blood (2008) 112 (11): 1868.

https://doi.org/10.1182/blood.V112.11.1868.1868

Published: 2008

Journal Articles

Increased Hepcidin Expression in Mice Affected by β-Thalassemia Reduces Iron Overload with No Effect on Anemia

Sara Gardenghi, PhD, Maria Franca Marongiu, Kristen Muirhead, Pedro Ramos, Cindy N. Roy, PhD, Nancy C. Andrews, MD, PhD, Elizabeta Nemeth, PhD, Antonia Follenzi, Eliezer Rachmilewitz, M.D, Patricia Giardina, MD, Robert W Grady, PhD, Stefano Rivella, PhD

Blood (2008) 112 (11): 128.

https://doi.org/10.1182/blood.V112.11.128.128

Published: 2008

Journal Articles

Body Composition and Its Relationship to Growth and Bone Mass in Patients with Thalassemia

Ellen Fung, PhD, Yan Xu, PhD, Janet Kwiatkowski, MD, Sylvia Titi Singer, MD, Ashutosh Lal, Maria G Vogiatzi, Nancy F. Olivieri, MD, Ellis J. Neufeld, Elliott Vichinsky, MD, Patricia Giardina, MD

Blood (2008) 112 (11): 3890.

https://doi.org/10.1182/blood.V112.11.3890.3890

Published: 2008

Journal Articles

Safety and Efficacy of Peginterferon Alfa-2a and Ribavirin for Hepatitis C in Thalassemia.

Paul Harmatz, MD, Nancy F. Olivieri, MD, Janet Kwiatkowski, MD, Elliott Vichinsky, MD, Patricia Giardina, MD, Farrukh Shah, MD, Elizabeth C. Wright, PhD, Roland Fischer, PhD, Maureen M. Jonas, MD

Blood (2006) 108 (11): 558.

https://doi.org/10.1182/blood.V108.11.558.558

Published: 2006

NARROW

Fracture Prevalence in Adults with Transfusion-Dependent Thalassemia Is Related to Osteoporosis and Age

The Effect of Vitamin D Supplementation On Calcium Excretion in Thalassemia

Removal of Macrophages From the Erythroid Niche Impairs Stress Erythropoiesis but Improves Pathophysiology of Polycythemia Vera and Beta-Thalassemia

Transfusion Complications in Thalassemia: A Report From the Centers for Disease Control and Prevention (CDC)

Potential Therapeutic Applications of Jak2 Inhibitors in Beta-Thalassemia and Sickle Cell Disease,

Investigating the Role of Cytokines and Hepcidin in Anemia of Inflammation

The Human Ankyrin Insulator Supports Production of Therapeutic Levels of Adult Hemoglobin Following β-Globin Gene Transfer in Hematopoietic Cells Derived From Thalassemic and Sickle Cell Patients

Monitoring Cardiac Siderosis in Patients with Beta-Thalassemia Major on Various Chelation Regimens,

Changes In Health Status and Quality of Life In Adults with Thalassemia: Year 1 Report of the Thalassemia Longitudinal Cohort Study.

Therapeutic Transgene Expression From Genomic Safe Harbors In Patient-Specific Induced Pluripotent Stem Cells

The Palatability and Tolerability of Deferasirox (Exjade®) Taken with Meals, Different Liquids, or Crushed and Added to Food

Hepcidin as a Therapeutic Tool to Limit Iron Overload and Improve Anemia In β-Thalassemia

Changes In Health Status and Quality of Life In Parental Reports of Children with Thalassemia: Year 1 Report of the Thalassemia Longitudinal Cohort Study

Understanding Provider Barriers to Hydroxyurea Use for Pediatric Sickle Cell Disease

Genetics of HbF and HbF Response to Hydroxyurea In Pediatric Sickle Cell Disease: A Multi-Site Pilot Analysis of Candidate SNP Variants

Phenomenon of Pain In Thalassemia: A Prospective Analysis by the Thalassemia Clinical Research Network (TCRN)

Increased Nucleosomal DNA Fragmentation in Leukocytes of Thalassemia Patients.

Increased Hepcidin Expression in Mice Affected by β-Thalassemia Reduces Iron Overload with No Effect on Anemia

Body Composition and Its Relationship to Growth and Bone Mass in Patients with Thalassemia

Safety and Efficacy of Peginterferon Alfa-2a and Ribavirin for Hepatitis C in Thalassemia.

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American Society of Hematology

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American Society of Hematology

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